ENST00000258443.7:c.1286C>G
(EDAR)
MANE Select
|
ENSP00000258443.2:p.Ala429Gly
|
|
ENST00000258443.6:c.1286C>G
(EDAR)
|
ENSP00000258443.2:p.Ala429Gly
|
|
ENST00000376651.1:c.1382C>G
(EDAR)
|
ENSP00000365839.1:p.Ala461Gly
|
|
ENST00000409271.5:c.1382C>G
(EDAR)
|
ENSP00000386371.1:p.Ala461Gly
|
|
NM_022336.3:c.1286C>G
(EDAR)
|
NP_071731.1:p.Ala429Gly
|
|
XM_006712204.1:c.1382C>G
(EDAR)
|
XP_006712267.1:p.Ala461Gly
|
|
XM_011510502.1:c.1433C>G
(EDAR)
|
XP_011508804.1:p.Ala478Gly
|
|
XM_011510503.1:c.1337C>G
(EDAR)
|
XP_011508805.1:p.Ala446Gly
|
|
XM_011510504.1:c.713C>G
(EDAR)
|
XP_011508806.1:p.Ala238Gly
|
|
XM_011510502.2:c.1526C>G
(EDAR)
|
XP_011508804.2:p.Ala509Gly
|
|
XM_011510503.2:c.1430C>G
(EDAR)
|
XP_011508805.2:p.Ala477Gly
|
|
XM_017004623.2:c.8370+123922G>C
(RANBP2)
|
XP_016860112.1:n.8370+123922G>C
|
|
NM_022336.4:c.1286C>G
(EDAR)
MANE Select
|
NP_071731.1:p.Ala429Gly
|
|